High Frequency Chest Wall Oscillation ICD-10 Codes

Full list of Medicare approved ICD-10 Codes for AffloVest HFCWO

Medicare Requirements for Bronchiectasis:

1.) Required: CT Scan confirming diagnosis of bronchiectasis.
2.) Required: Daily productive cough for at least 6 continuous months.
Frequent (i.e. more than 2/year) exacerbations requiring antibiotic therapy.
3.) Required: Documentation (chart notes) of another treatment (flutter valve,
percussion, postural drainage, breathing techniques, suctioning) tried to mobilize
secretions and clearly indicating the other technique or device has failed.

ICD-10 Code  Description
J47.0 Bronchiectasis with acute lower respiratory infection
J47.1  Bronchiectasis with (acute exacerbation
J47.9  Bronchiectasis, uncomplicated
Q33.4 Congenital Bronchiectasis

Medicare Requirements for Other Respiratory Disorders, Cystic Fibrosis and Neuromuscular Conditions:

Physicians order that includes: AffloVest prescription, qualifying Dx, chart notes to support the Dx, and well-documented failure of standard treatments to adequately mobilize retained secretions.

ICD-10 Code  Description 
Disorders of diaphragm
E84.0 Cystic Fibrosis with Pulmonary Manifestations
E84.9 Cystic Fibrosis, unspecified
A15.0 Tuberculosis of lung
B91 Sequelae of Poliomyelitis
D84.1 Defects in the complement system
D81.810 Biotinidase deficiency
D81.82 Activated phosphoinositide 3-kinase delta syndrome [apds]
G12.0 Infantile spinal muscular atrophy, type I (Werdnig-Hoffman)
G12.1 Other inherited spinal muscular atrophy
G12.20 Motor neuron disease, unspecified
G12.21 Amyotrophic lateral sclerosis
G12.22 Progressive bulbar palsy
G12.23 Primary lateral sclerosis
G12.24 Familial motor neuron disease
G12.25 Progressive spinal muscle atrophy
G12.29 Other motor neuro disease
G12.8 Other spinal muscular atrophies and related syndromes
G12.9 Spinal muscular atrophy, unspecified
G14 Postpolio syndrome
G35 Multiple sclerosis
G71.00 Muscular dystrophy, unspecified
G71.01 Duchenne or Becker muscular dystrophy
G71.02 Facioscapulohumeral muscular dystrophy
G71.031 Autosomal dominant limb girdle muscular dystrophy
G71.032 Myotonic muscular dystrophy
G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction
G71.0340 Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unsp
G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
G71.038 Other limb girdle muscular dystrophy
G71.039 Limb girdle muscular dystrophy, unspecified
G71.09 Other specified muscular dystrophies
G71.11 Myotonic muscular dystrophy
G71.12 Myotonia congenita
G71.13 Myotonic chondrodystrophy
G71.14 Drug induced myotonia
G71.19 Other specified myotonic disorders
G71.2 Congenital myopathies
G71.21 Nemaline myopathy
G71.220 X-linked myotubular myopathy
G71.228 Other centronuclear myopathy
G71.29 Other congenital myopathy
G71.3 Mitochondrial myopathy not elsewhere classified
G71.8 Other primary disorders of muscles
G72.0 Drug-induced myopathy
G72.1 Alcoholic myopathy
G72.2 Myopathy due to other toxic agents
G72.89 Other specified myopathies
G73.7 Myopathy in diseases classified elsewhere
G80.0 Spastic quadriplegic cerebral palsy
G82.50 Quadriplegia, unspecified
G82.51 Quadriplegia, C1-C4 complete
G82.52 Quadriplegia, C1-C4 incomplete
G82.53 Quadriplegia, C5-C7 complete
G82.54 Quadriplegia, C5-C7 incomplete
M32.82 Systemic sclerosis with myopathy
M33.02 Juvenile dermatopolymyositis with myopathy
M33.12 Other dermatopolmyositis with myopathy
M33.22 Polymyositis with myopathy
M33.92 Dermatopolymyositis, unspecified with myopathy
M34.82 Systemic sclerosis with myopathy
M35.03 Sicca syndrome with myopathy